Users can query the SNP information according to the gene ID.


Gene ID

Results: 1 - 13 of 13 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA05g42310 A05 40164615 G A missense_variant MODERATE c.3293C>T|p.Ser1098Phe S53
2 BAA05g42310 A05 40164678 C T missense_variant MODERATE c.3230G>A|p.Gly1077Glu S232
3 BAA05g42310 A05 40164805 C T missense_variant MODERATE c.3103G>A|p.Ala1035Thr S306
S308
4 BAA05g42310 A05 40165362 G A missense_variant MODERATE c.2546C>T|p.Ser849Phe S242
5 BAA05g42310 A05 40166318 G A synonymous_variant LOW c.1677C>T|p.Phe559Phe S185
6 BAA05g42310 A05 40166420 C T splice_acceptor_variant&intron_variant HIGH c.1576-1G>A| S221
7 BAA05g42310 A05 40168331 C T upstream_gene_variant MODIFIER c.-1G>A| S221
8 BAA05g42310 A05 40169937 G A upstream_gene_variant MODIFIER c.-1607C>T| S64
9 BAA05g42310 A05 40171653 C T upstream_gene_variant MODIFIER c.-3323G>A| S18
S221
S293
S294
10 BAA05g42310 A05 40171936 C T upstream_gene_variant MODIFIER c.-3606G>A| S192
11 BAA05g42310 A05 40172073 C T upstream_gene_variant MODIFIER c.-3743G>A| S226
12 BAA05g42310 A05 40173211 C T upstream_gene_variant MODIFIER c.-4881G>A| S151
S263
13 BAA05g42310 A05 40173275 C T upstream_gene_variant MODIFIER c.-4945G>A| S295